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May 5, 2003
Volume 81, Number 18
CENEAR 81 18
ISSN 0009-2347 |
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REALITY CHECK
When Chemistry Bows To Economics
To prepare chiral molecules, asymmetric synthesis is, in principle, the best way forward, according to Joel M. Hawkins, a research adviser at Pfizer Global Research & Development. He spoke last March on the use of asymmetric catalysis in the pharmaceutical industry at an American Chemical Society ProSpectives meeting held in Boston. But the bottom line is always economics, he emphasized, as he described efforts to manufacture candoxatril, a drug Pfizer had been developing to treat congestive heart failure.
A key building block is a chiral glutarate derivative. Initially, the required S enantiomer was obtained through classical resolution of the racemate using pseudoephedrine. As candoxatril progressed through the pipeline, more efficient asymmetric syntheses were explored.
Asymmetric hydrogenation of the alkene precursor with ruthenium-BINAP gives the required product in up to 94% enantiomeric excess (ee), but in low yield. Up to 30% of the substrate is isomerized to enol by-products. A rhodium-MeDuPHOS system yields the desired enantiomer in 95% yield and greater than 99% ee [J. Org. Chem., 64, 3290 (1999)].
But when it came to prepare two tons of the the drug for Phase III clinical trials, Pfizer switched to a ruthenium-MeOBIPHEP system. With lower yields because of isomerization and with lower enantiomeric excess, this system was inferior to rhodium-MeDuPHOS. However, the catalyst availability and licensing agreement were more favorable with ruthenium-MeOBIPHEP. "The business aspect and the chemical aspect were in competition, and the business aspect won," Hawkins said. Process improvements by researchers at PPG-Sipsy decreased the isomerization to tolerable levels and made the reaction reasonable on a large scale [Org. Process Res. Dev., 5, 438 (2001).]
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COVER STORY
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CHIRAL BUSINESS
Fine chemicals companies are jockeying for position to deliver the increasingly complicated chiral small molecules of the future
CONTEST
Vying For Chiral Hydroformylation Advantage
NICHE PLAYER
Chiral Quest Sees Advantages In Independence
STEADY SHARE
Worldwide sales of single-enantiomer pharmaceutical products approach $160 billion
BLOCKBUSTERS
Top 10 single-enantiomer products belong to billion-dollar club
HARVEST
Research in Chiral Fine Chemicals Reaps Recognition
CONSTANT
Chiral separations are enduring items in the toolbox
CASE HISTORIES
History and choice shape portfolios
CALENDAR
Events Of Interest
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Chemical & Engineering News
Copyright © 2003 American Chemical Society |
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COVER STORY
|
CHIRAL BUSINESS
Fine chemicals companies are jockeying for position to deliver the increasingly complicated chiral small molecules of the future
CONTEST
Vying For Chiral Hydroformylation Advantage
NICHE PLAYER
Chiral Quest Sees Advantages In Independence
STEADY SHARE
Worldwide sales of single-enantiomer pharmaceutical products approach $160 billion
BLOCKBUSTERS
Top 10 single-enantiomer products belong to billion-dollar club
CHIRALITY AT WORK
Drug developers can learn much from recent successful and failed chiral switches
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